Canonical Allele Identifier: PA2828029049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676783
ClinVar RCV Id: RCV003470242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2302Glu
CA16038170
NM_001354906.2:c.6904A>G